|Publication number||US6548418 B2|
|Application number||US 10/158,249|
|Publication date||Apr 15, 2003|
|Filing date||May 30, 2002|
|Priority date||Feb 26, 1998|
|Also published as||US6420777, US6680259, US20010013638, US20020145179, US20030207586|
|Publication number||10158249, 158249, US 6548418 B2, US 6548418B2, US-B2-6548418, US6548418 B2, US6548418B2|
|Inventors||Chung Hon Lam, Eric Seung Lee, Francis Roger White|
|Original Assignee||International Business Machines Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (7), Non-Patent Citations (5), Referenced by (10), Classifications (15), Legal Events (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a divisional of application Ser. No. 09/031,251, filed Feb. 26, 1998, now U.S. Pat. No. 6,420,777.
This invention relates generally to the manufacture of integrated circuit (I/C) chips and particularly to the fabrication or processing of a silicon substrate to form the circuitry for the I/C chip. During one stage of manufacture of I/C chips, a silicon dioxide layer is applied over a silicon substrate. The silicon dioxide must be etched at various places to provide openings to the substrate for electrical connections. One conventional technique of etching is by means of reactive ion etching (RIE). With reactive ion etching it is conventional to provide an etch stop barrier between the silicon substrate and the silicon dioxide layer formed thereon. One conventional etch stop barrier is silicon nitride (SixNy). These silicon nitride barriers are conventionally deposited by low pressure chemical vapor deposition (LPCVD) utilizing conventional equipment. In one embodiment mixtures of silane (SiH4) and ammonia (NH3) are utilized as an ambient to provide the necessary silicon and nitrogen moieties for the formation of the silicon nitride.
However, it has been found in the past that there were variations from process to process of forming the SixNy barrier in the effectiveness of the nitride barrier in its selectivity with respect to SiO2 when reactive ion etching the SiO2. When etching SiO2 it is desirable to have as much selectivity as possible of the etch stop with respect to the SiO2 so as to allow a minimum thickness of the etch stop to be applied. It was also found that there were variations in the resulting barrier in the effectiveness of the silicon nitride to prevent passing of positive mobile ions (PMI) which may occur during subsequent processing due primarily to contaminants introduced into the SiO2 layer. Positive mobile ion contamination (PMIC) such as in a gate oxide of CMOS devices must be reduced to a minimum. Thus a requirement of the silicon nitride barrier is that it act to effectively block positive mobile ions from penetrating into the substrate during subsequent processing steps.
Therefore it is desirable to provide a silicon nitride barrier that is both highly selective to etching of SiO2 and also effective to block the passage of positive mobile ions in subsequent processing steps.
According to the present invention, a method for reactive ion etching of SiO2 with an etch stop barrier for use in such an etching is provided. It has been found that a silicon nitride (SixNy) barrier having a Six to Ny ratio (x:y) of less than about 0.8 and preferably the stoichiometric amount of 0.75 provides excellent resilience to positive mobile ion contamination, but poor etch selectivity. However, a silicon nitride barrier having a ratio of Six to Ny (x:y) of 1.0 or greater has excellent etch selectivity with respect to SiO2 but a poor barrier to positive mobile ion contamination. The technique of the present invention includes providing a substrate which conventionally is a doped silicon substrate, and forming a barrier of silicon nitride on the substrate which barrier has two sections or layers. One section has a greater etch selectivity with respect to silicon dioxide than the second section and the second section has a greater resistance to transmission of positive mobile ions than the first section. Preferably the two sections are formed by forming one section, referred to as the lower section adjacent to silicon substrate with a silicon to nitrogen ratio of less than about 0.8 and preferably about 0.75 which is the stoichiometric ratio of silicon to nitrogen. The second section, or upper section is preferably formed with the ratio of the silicon to nitrogen of greater than about 0.8 and preferably at least about 1.0. Preferably the two sections together are from about 50 to about 100 nanometers thick and in the preferred embodiment, each section is about 25 to 50 nanometers thick.
FIG. 1 is a graph of the etch rate of silicon nitride (SixNy) in Ar:CHF3CF4 at various silicon to nitrogen ratios (x:y) of the silicon nitride;
FIG. 2 is a bar graph showing the Vt shift of a substrate after reactive ion etching using silicon nitride (SixNy) barriers of various ratios of silicon to nitrogen (x:y);
FIG. 3 is a graph similar to FIG. 2 graphing the positive ion density in the substrate as a function of the ratio of the silicon to nitrogen (x:y) in silicon nitride; and
FIGS. 4A through 4G show the steps of the method of the present invention somewhat diagrammatically.
The use of silicon nitride as an etch stop barrier is well known in the art especially for stopping the etch during reactive ion etching (RIE) of silicon dioxide disposed over a silicon or doped silicon substrate in the manufacture of integrated circuit chips. Reactive ion etching is used in chip manufacturing to form openings through the silicon dioxide so as to provide access to the substrate. Typically the opening will be filled with metal such as tungsten or other metal as is well known. In etching the silicon dioxide an etch stop layer is used so as to allow the etching to stop or essentially terminate once the etching has penetrated through the silicon dioxide layer. Expressed another way, when the etching has pierced the silicon dioxide layer it is desired that the etching not continue to any significant extent. The barrier layer of etch stop material is to ensure that the etch stops substantially uniformly at all the various locations being etched through the silicon dioxide. Thus, one of the principal requirements of the etch stop material is that it have a relatively high selectivity of etching with respect to the material which is intended to be etched i.e. silicon dioxide. Expressed another way, once the silicon dioxide has been etched it is desirable that there be very little etching taking place after that.
FIG. 1 shows the etching rate of SixNy in nanometers per minute using an AME 5000 tool with Ar:CHF3 atmosphere at various ratios of silicon to nitrogen in a silicon nitride (SixNy) barrier. As can be seen, when the ratio of silicon to nitrogen is 0.75 (which is the stoichiometric ratio) the etch rate is between 140 and 160 nanometers per minute, but as the ratio of silicon to nitrogen increases, this etch rate decreases dramatically to a point where when the ratio of Si to N is about 1.0 the etch rate has dropped down to about 20 nanometers per minute. With a ratio greater than 1.0 no improvement in the etch rate resistance is achieved. Thus, based on this particular characterization, in order to get the lowest etch rate of silicon nitride and thus the highest etch selectivity, it is desirable to have a ratio of silicon to nitrogen of at least about 1.0.
However, in subsequent processing during chip manufacture there can be generated positive mobile ions (PMI), in particular Na+ and K+, principally from contamination in the SiO2 layer. If these positive ions diffuse even in small amounts into the silicon substrate they can cause significant degradation of the substrate material in some structures. Thus, it is desirable and often even necessary that these ions be essentially excluded from penetrating the barrier and diffusing into the substrate. FIGS. 2 and 3 show the amount of diffusion of positive mobile ions especially sodium (Na+) as measured by Vt Shift (mV) shown in FIG. 2 and ion density in 1010 Ions/cm2 shown in FIG. 3 in substrates with SixNy nitride barriers having various ratios of Si to N in the silicon nitride. At a Si to N ratio of 1.05 there is a very high number of mobile ions passing through the silicon nitride barrier, and even at a ratio of 1.0 there is an appreciable amount of these ions penetrating; indeed even at a ratio of silicon to nitrogen of 0.8 there is a significant amount of PMIC (positive mobile ion contamination). It is not until the ratio of silicon to nitrogen is 0.75 (i.e. the stoichiometric ratio) that the PMIC is essentially eliminated.
Thus, if one were to design the barrier to maximize resistance to positive mobile ion penetration one would use a ratio of silicon to nitrogen of 0.75. However, as shown above, this would provide very poor etch selectivity. On the other hand, if one were to design for the best etch selectivity, one would design a nitride barrier having a ratio of silicon to nitrogen of 1.0 or greater; but this would provide poor resistance to positive mobile ion penetration.
According to the present invention, a barrier is provided which will achieve both high resistance to positive mobile ion penetration and very good etch selectivity with respect to SiO2. This is accomplished by providing a barrier having two separate sections or layers. A first layer of silicon nitride is tailored to have excellent resistance to positive mobile ion penetration and thus has a ratio of silicon to nitrogen of less than about 0.8 and preferable about 0.75. A second layer of silicon nitride is provided which has a silicon to nitrogen ratio of greater than about 0.8 preferably about 1.05. This will provide excellent etch selectivity. By having a dual layer barrier as described, the barrier will provide not only good etch selectivity but resistance to positive mobile ion contamination.
Referring now to FIGS. 4A through 4G, various steps of the present invention are depicted in very diagrammatic fashion. As seen in FIG. 4A a silicon substrate 10 is provided which has a gate device 12 separated from the substrate 10 by means of a gate oxide layer 13. The substrate has a region 14 of opposite polarity (shown as N+) on top of which is a silicided layer 15, which silicided layer 15 also overlies the gate 12.
A first layer of silicon nitride (SixNy) 16 is deposited over the substrate 10 and the gate device 12. The first layer of silicon nitride 16 in the preferred embodiment is formed in an AME 5000 tool sold by Applied Materials, Inc. with an atmosphere of SiH4 and NH3 to form a silicon nitride having a ratio of silicon to nitrogen of about 0.75. The ratio of silicon to nitrogen is controlled by controlling the ratio of SiH4 to NH3 in a well known manner. Preferably this first layer 16 is from about 25 to about 50 nanometers thick.
Following the deposition of the first layer 16 a second layer 18 of silicon nitride is deposited over the first layer 16 as shown in FIG. 4B. Again this is done in the AME 5000 tool in an atmosphere of SiH4 and NH3. The ratio of SiH4 to NH3 in forming this second layer 18 is controlled so as to form a silicon nitride with silicon to nitrogen ratio of at least 1.0 and preferably 1.05. This layer 18 is also formed to a thickness of about 25 to about 50 nanometers so that the total thickness of the first and second layers 16, 18 is from about 50 to about 100 nanometers. It is not critical whether the layer 16 or 18 is formed on the substrate; however in the preferred embodiment, the layer 16 is formed on the substrate 10 and the layer 18 is formed over the layer 16.
On top of the layer 18 is deposited a layer of silicon dioxide (TEOS) 20 preferably doped with boron (BSG) or phosphorous (PSG) or both (BPSG) as shown in FIG. 4C which also is formed in a conventional manner again using the AME 5000 tool. This layer 20 is conventionally at least about 0.6 microns thick.
As shown in FIG. 4D surface 22 of the TEOS 20 is coated with a photoresist 24, which is photoimaged and developed in a conventional manner to provide openings one of which is shown at 26 in the photoresist 22. One photoresist that is especially useful is positive acting resist 5409 sold by Shipley Corp.
Following the developing of the photoresist layer 24, the SiO2 exposed through the opening 26 is anisotropically etched preferably in a CHF3:O2 atmosphere to form opening 28 in the SiO2 as shown in FIG. 4E. Because of the layer 18 of SixNy has a high Si to N ratio it has a very high selectivity of etch rate as compared to the silicon dioxide 20, the layer 18 SixNy acts as an excellent etch stop material. Never-the-less a certain amount of the layer 18 is removed as shown as 29 in FIG. 4E.
Following the reactive ion etching, the remaining photoresist 24 is stripped and the exposed silicon nitride layers 16 and 18 are removed by dry etching in Ar:CHF3 to provide the structures shown in FIG. 4F.
Following the removal of the SixNy layers in openings 26, a contact barrier such as TiN 30 is formed on the SiO2 wall in opening 26 and surface 22 and on the exposed substrate 10. This is followed by deposition of a metal such as Tungsten (W) 32, as shown in FIG. 4G.
That portion of the SixNy layers remaining under the SiOx, which have not been exposed and etched, contain the layer 16 which has excelled resistance to PMIC during subsequent processing. Thus the two layers 16 and 18 have together provided high etch selectivity during RIE of the silicon and also reduced or eliminating PMIC during subsequent processing.
Of course it should be understood that the ratios of Si to N in the two layers can be varied as can be the thicknesses of the two layers. For example if there is more concern for either more etch selectivity or improved barrier to positive mobile ion penetration the thickness of each of the layers 16 and 18 as well as the ratios of Si to N in each layer can be varied. Also, as noted above the layer 18 with high etch selectivity can be formed on the substrate, and the layer 16 with good resistance to PMIC can be formed on the layer 18.
Also it should be understood that in using a conventional tool for forming the silicon nitride, it is possible to provide a barrier which has a gradient throughout; i.e. a structure which at the surface of the substrate has excellent barrier properties to positive mobile ion penetration and then gradually increases the silicon to nitrogen ratio so that the outer surface has high etch selectivity (or vice versa). This can be accomplished by starting with a ratio of SiH4 to NH3 that will provide a ratio of 0.75 of Si to N in the silicon nitride, and then gradually changing the concentrations of SiH4 and NH3 such that at the end of the cycle the ratio of Si to N in the silicon nitride is 1.0 or more.
Thus, according to the present invention an improved etch stop barrier is provided which provides both excellent resistance to positive mobile ion penetration and also very good etched selectivity in the same barrier by having multiple layers of material which are tailored to a specific function.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4342617 *||Feb 23, 1981||Aug 3, 1982||Intel Corporation||Process for forming opening having tapered sides in a plasma nitride layer|
|US5444653 *||Apr 13, 1994||Aug 22, 1995||Sanyo Electric Co., Ltd.||Semiconductor memory device with stack type memory cell|
|US5459354 *||Dec 20, 1993||Oct 17, 1995||Nippon Steel Corporation||Semiconductor device with improved insulation of wiring structure from a gate electrode|
|US5702989 *||Feb 8, 1996||Dec 30, 1997||Taiwan Semiconductor Manufacturing Company Ltd.||Method for fabricating a tub structured stacked capacitor for a DRAM cell having a central column|
|US5811357 *||Mar 26, 1997||Sep 22, 1998||International Business Machines Corporation||Process of etching an oxide layer|
|US5897372 *||Nov 1, 1995||Apr 27, 1999||Micron Technology, Inc.||Formation of a self-aligned integrated circuit structure using silicon-rich nitride as a protective layer|
|US5940732 *||Nov 25, 1996||Aug 17, 1999||Semiconductor Energy Laboratory Co.,||Method of fabricating semiconductor device|
|1||"1994 ieee international reliability physics proceedings", 1994, Institute of Electrical and Electronic Engineers, Inc. (4 pages).|
|2||"1994 International Integrated Reliability Workshop Final Report", Stanford Sierra Camp, Lake Tahoe, California, Oct. 16-19, 1994. (2 pages).|
|3||"Characterization of Plasma-Enhanced Chemical Vapor Deposited Nitride Films Used in Very Large Scale Integrated Applications", A.K. Stamper and S.L. Pennington, J. Electrochem, Soc., vol. 140, No. 6, Jun. 1993. Pages 1748-1752.|
|4||"Ion Transport Phenomena in Insulating Films", E.H. Snow, A.S. Grove, B.E. Deal, and C.T. San, Journal of Applied Physics. vol. 30., pp. 1664-1671.|
|5||"Thin Film of Lithium Nioblum Oxynitride as Ionic Conductor", Le Quang Nguyen and Vo-Van Truong, 1996, American Institute of Physics, pp. 2914-2917.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US6680259 *||Apr 14, 2003||Jan 20, 2004||International Business Machines Corporation||Dual layer etch stop barrier|
|US7381660 *||Nov 19, 2003||Jun 3, 2008||Advanced Micro Devices, Inc.||Dielectric barrier layer for a copper metallization layer having a varying silicon concentration along its thickness|
|US8653580 *||Sep 14, 2012||Feb 18, 2014||Samsung Electronics Co., Ltd.||Semiconductor devices and methods of fabricating the same|
|US8872311 *||Feb 13, 2004||Oct 28, 2014||Agere Systems Inc.||Semiconductor device and a method of manufacture therefor|
|US20030207586 *||Apr 14, 2003||Nov 6, 2003||International Business Machines Corporation||Dual layer etch stop barrier|
|US20040152333 *||Nov 19, 2003||Aug 5, 2004||Larry Zhao||Dielectric barrier layer for a copper metallization layer having a varying silicon concentration along its thickness|
|US20050179115 *||Feb 13, 2004||Aug 18, 2005||Agere Systems Inc.||Semiconductor device and a method of manufacture therefor|
|US20080079083 *||Oct 31, 2007||Apr 3, 2008||Agere Systems Inc.||Semiconductor device and a method of manufacture therefor|
|US20090108359 *||Oct 31, 2007||Apr 30, 2009||Agere Systems Inc.||A semiconductor device and method of manufacture therefor|
|US20130009213 *||Sep 14, 2012||Jan 10, 2013||Samsung Electronics Co., Ltd.||Semiconductor devices and methods of fabricating the same|
|U.S. Classification||438/723, 438/740, 438/724, 257/E21.252, 438/970, 438/637, 438/634, 257/E21.293|
|International Classification||H01L21/311, H01L21/318|
|Cooperative Classification||Y10S438/97, H01L21/31116, H01L21/3185|
|European Classification||H01L21/311B2B, H01L21/318B|
|Nov 1, 2006||REMI||Maintenance fee reminder mailed|
|Apr 15, 2007||LAPS||Lapse for failure to pay maintenance fees|
|Jun 12, 2007||FP||Expired due to failure to pay maintenance fee|
Effective date: 20070415
|Sep 3, 2015||AS||Assignment|
Owner name: GLOBALFOUNDRIES U.S. 2 LLC, NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:INTERNATIONAL BUSINESS MACHINES CORPORATION;REEL/FRAME:036550/0001
Effective date: 20150629
|Oct 5, 2015||AS||Assignment|
Owner name: GLOBALFOUNDRIES INC., CAYMAN ISLANDS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:GLOBALFOUNDRIES U.S. 2 LLC;GLOBALFOUNDRIES U.S. INC.;REEL/FRAME:036779/0001
Effective date: 20150910